WEE1 WEE1 G2 checkpoint kinase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 68 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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70 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | WEE1A |
SYNONYM | WEE1hu |
MIM | 193525 OMIM |
HGNC | HGNC:12761 HGNC |
Ensembl | ENSG00000166483 Ensembl |
AllianceGenome | HGNC:12761 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000450114.7 | hg38 | chr11 | 9,573,670 | 9,589,985 | 16,316 |
ENST00000681684.1 | hg38 | chr11 | 9,575,496 | 9,589,622 | 14,127 |
ENST00000530712.6 | hg38 | chr11 | 9,581,227 | 9,589,985 | 8,759 |
ENST00000299613.10 | hg38 | chr11 | 9,574,687 | 9,589,984 | 15,298 |
ENST00000450114.7 | hg19 | chr11 | 9,595,217 | 9,611,532 | 16,316 |
ENST00000299613.10 | hg19 | chr11 | 9,596,234 | 9,611,531 | 15,298 |
ENST00000681684.1 | hg19 | chr11 | 9,597,043 | 9,611,169 | 14,127 |
ENST00000530712.6 | hg19 | chr11 | 9,602,774 | 9,611,532 | 8,759 |
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